HydroPICC
K-Number: K172885 · 2018-02-20
Device Summary
Frequently Asked Questions
What is the HydroPICC?
HydroPICC is a medical device that received FDA 510(k) clearance on 2018-02-20. The listed applicant is Access Vascular, Inc.. The 510(k) number is K172885.
When did HydroPICC receive FDA 510(k) clearance?
HydroPICC received FDA 510(k) clearance on 2018-02-20, under 510(k) number K172885.
Who is the listed applicant for HydroPICC?
The FDA 510(k) record lists Access Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HydroPICC?
The FDA product code for HydroPICC is LJS.
Other records listing Access Vascular, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LJS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.